T2405 |
Revaprazan hydrochloride
|
178307-42-1
|
99.64%
|
|
Revaprazan hydrochloride (YH1885) is the hydrochloride salt form of a lipophilic, weak base with potassium-competitive acid blocking (P-CAB) activity.
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T22790 |
FR 122047
|
130717-51-0
|
99.63%
|
|
FR 122047 (1-[(4,5-Bis(4-methoxyphenyl-2-thiazoyl)carbonyl]-4-methylpiperazine, Hydrochloride) is a potent and selective inhibitor of COX-1 with IC50 of 28 nM an...
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T9042 |
Teriflunomide impurity 3
|
1011244-72-6
|
99.62%
|
|
Teriflunomide impurity 3 (4-Amino-N-(4-trifluoromethylphenyl)benzamide) is a selective COX-1 inhibitor(IC50 of 30 μM). It is less active against COX-2 (IC50>100 ...
|
TN1723 |
Hamaudol
|
735-46-6
|
99.62%
|
|
Hamaudol is a chromone isolated from Saposhnikovia divaricata,has analgesic and anti-inflammary activities, it showed inhibitory activity on COX-1 and COX-2 acti...
|
T0705 |
Triflusal
|
322-79-2
|
99.61%
|
|
Triflusal (UR1501) is a 2-acetoxy-4-trifluoromethylbenzoic acid and it is an aspirin chemically-related molecule but not a derivative.
|
TN1273 |
7,4'-Dihydroxyflavone
|
2196-14-7
|
99.6%
|
|
7,4'-Dihydroxyflavone (4',7-Dihydroxyflavone) can induce transcription of nodulation (nod) genes in Rhizobium meliloti. It has inhibitory activities against COX-...
|
T0758 |
Piroxicam
|
36322-90-4
|
99.59%
|
|
Piroxicam (CP-16171) is a non-specific COX inhibitor.
|
TN1377 |
α-Spinasterol
|
481-18-5
|
99.58%
|
|
α-Spinasterol is a transient receptor potential vanilloid 1 (TRPV1) antagonist, has anti-inflammatory, antidepressant, antioxidant and antinociceptive effects. α...
|
T0498 |
Salsalate
|
552-94-3
|
99.57%
|
|
Salsalate (Sasapyrine) is an orally available salicylate and non-steroidal anti-inflammatory drug (NSAID), with anti-inflammatory, analgesic and antipyretic acti...
|
T0319 |
Suxibuzone
|
27470-51-5
|
99.56%
|
|
Suxibuzone (Suxibuzona) is a drug used for joint and muscular pain. It is a prodrug of the non steroidal anti inflammatory drug phenylbutazone, and is commonly u...
|
T0477 |
Zileuton
|
111406-87-2
|
99.56%
|
|
Zileuton (A 64077) is a synthetic derivative of hydroxyurea with antiasthmatic properties. The leukotriene inhibitor zileuton blocks 5-lipoxygenase, which cataly...
|
T62061 |
COX-2-IN-6
|
2756347-91-6
|
99.56%
|
|
COX-2-IN-6 is a potent, selective, and orally available cyclooxygenase-2 (COX-2) inhibitor with an IC50 of 0.84 μM and a Ki of 69 nM.COX-2-IN-6 inhibits COX-2-dr...
|
TN3500 |
Beta-Amyrone
|
638-97-1
|
99.55%
|
|
beta-Amyrone (β-Amyron) has antifungal activity against Chikungunya virus replication with an EC50 of 86 uM. beta-Amyrone has anti-inflammatory activity through ...
|
T0888 |
Felbinac
|
5728-52-9
|
99.55%
|
|
Felbinac (Dapson), a topical medicine, is an active metabolite of fenbufen. It is belonging to the family of medicines known as non-steroidal anti-inflammatory d...
|
T2758 |
Madecassic acid
|
18449-41-7
|
99.55%
|
|
Madecassic acid (L-fucopyranose) is extracted from the whole herb of Centella asiatica.
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T0212 |
Seratrodast
|
112665-43-7
|
99.54%
|
|
Seratrodast (ABT-001) (INN), a thromboxane A2 (TXA2) receptor (TP receptor) antagonist, is mainly used in the therapy of asthma. It was the first TP receptor ant...
|
T0798 |
Triamcinolone
|
124-94-7
|
99.54%
|
|
Triamcinolone (Aristocort) is a synthetic glucocorticoid with anti-inflammatory and immunomodulating properties. Upon cell entry, triamcinolone binds to and acti...
|
T3805 |
Prim-O-glucosylcimifugin
|
80681-45-4
|
99.54%
|
|
Prim-O-glucosylcimifugin (Cimifugin 7-glucoside) can inhibit the proliferation of SMC(smooth muscle cell) stimulated by TNF-alpha, increase the proportion of G0/...
|
T1468 |
Lornoxicam
|
70374-39-9
|
99.53%
|
|
Lornoxicam (Chlortenoxicam) (chlortenoxicam) is a new nonsteroidal anti-inflammatory drug (NSAID) of the oxicam class with analgesic, anti-inflammatory, and anti...
|
T0459 |
Sulindac
|
38194-50-2
|
99.49%
|
|
Sulindac (Sulindac sulfoxide) is a sulfinylindene derivative prodrug with potential antineoplastic activity. Converted in vivo to an active metabolite, sulindac,...
|